A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428693



Internal ID21086246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145220601..145225300hg38UCSC Ensembl
chr7:144917694..144922393hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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